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Behavior of bacteriome symbionts during transovarial transmission and development of the Asian citrus psyllid

The Asian citrus psyllid Diaphorina citri Kuwayama (Hemiptera: Liviidae) is a serious pest worldwide, transmitting Candidatus Liberibacter spp. (Alphaproteobacteria), the causative agents of a devastating citrus disease known as huanglongbing or greening disease. In a symbiotic organ called the bact...

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Autores principales: Dan, Hiroki, Ikeda, Naoya, Fujikami, Masaya, Nakabachi, Atsushi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5730177/
https://www.ncbi.nlm.nih.gov/pubmed/29240843
http://dx.doi.org/10.1371/journal.pone.0189779
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author Dan, Hiroki
Ikeda, Naoya
Fujikami, Masaya
Nakabachi, Atsushi
author_facet Dan, Hiroki
Ikeda, Naoya
Fujikami, Masaya
Nakabachi, Atsushi
author_sort Dan, Hiroki
collection PubMed
description The Asian citrus psyllid Diaphorina citri Kuwayama (Hemiptera: Liviidae) is a serious pest worldwide, transmitting Candidatus Liberibacter spp. (Alphaproteobacteria), the causative agents of a devastating citrus disease known as huanglongbing or greening disease. In a symbiotic organ called the bacteriome, D. citri possesses an organelle-like defensive symbiont, Candidatus Profftella armatura (Betaproteobacteria), and a nutritional symbiont, Ca. Carsonella ruddii (Gammaproteobacteria). Drastically reduced symbiont genomes and metabolic complementarity among the symbionts and D. citri indicate their mutually indispensable association. Moreover, horizontal gene transfer between the Profftella and Liberibacter lineages suggests ecological and evolutionary interactions between the bacteriome symbiont and the HLB pathogen. Using fluorescence in situ hybridization, we examined the behavior of Profftella and Carsonella during transovarial transmission and the development of D. citri. In the bacteriomes of sexually-mature female adults, symbionts transformed from an extremely elongated tubular form into spherical or short-rod forms, which migrated toward the ovary. The symbionts then formed mosaic masses, which entered at the posterior pole of the vitellogenic oocytes. After anatrepsis, Carsonella and Profftella migrated to the central and peripheral parts of the mass, respectively. Following the appearance of host nuclei, the mass cellularized, segregating Carsonella and Profftella in the central syncytium and peripheral uninucleate bacteriocytes, respectively. Subsequently, the uninucleate bacteriocytes harboring Profftella assembled at the posterior pole, while the syncytium, containing Carsonella, sat on the anterior side facing the germ band initiating katatrepsis. During dorsal closure, the syncytium was divided into uninuclear bacteriocytes, which surrounded the mass of bacteriocytes containing Profftella. Once fully surrounded, the bacteriocyte mass containing Profftella was fused into a syncytium. Prior to hatching, a pair of wing-like protrusions arose from both lateral sides of the bacteriome, which continued to grow throughout the nymphal stages. These findings provide a foundation for better understanding the intricate relationship between D. citri and its microbiota.
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spelling pubmed-57301772017-12-22 Behavior of bacteriome symbionts during transovarial transmission and development of the Asian citrus psyllid Dan, Hiroki Ikeda, Naoya Fujikami, Masaya Nakabachi, Atsushi PLoS One Research Article The Asian citrus psyllid Diaphorina citri Kuwayama (Hemiptera: Liviidae) is a serious pest worldwide, transmitting Candidatus Liberibacter spp. (Alphaproteobacteria), the causative agents of a devastating citrus disease known as huanglongbing or greening disease. In a symbiotic organ called the bacteriome, D. citri possesses an organelle-like defensive symbiont, Candidatus Profftella armatura (Betaproteobacteria), and a nutritional symbiont, Ca. Carsonella ruddii (Gammaproteobacteria). Drastically reduced symbiont genomes and metabolic complementarity among the symbionts and D. citri indicate their mutually indispensable association. Moreover, horizontal gene transfer between the Profftella and Liberibacter lineages suggests ecological and evolutionary interactions between the bacteriome symbiont and the HLB pathogen. Using fluorescence in situ hybridization, we examined the behavior of Profftella and Carsonella during transovarial transmission and the development of D. citri. In the bacteriomes of sexually-mature female adults, symbionts transformed from an extremely elongated tubular form into spherical or short-rod forms, which migrated toward the ovary. The symbionts then formed mosaic masses, which entered at the posterior pole of the vitellogenic oocytes. After anatrepsis, Carsonella and Profftella migrated to the central and peripheral parts of the mass, respectively. Following the appearance of host nuclei, the mass cellularized, segregating Carsonella and Profftella in the central syncytium and peripheral uninucleate bacteriocytes, respectively. Subsequently, the uninucleate bacteriocytes harboring Profftella assembled at the posterior pole, while the syncytium, containing Carsonella, sat on the anterior side facing the germ band initiating katatrepsis. During dorsal closure, the syncytium was divided into uninuclear bacteriocytes, which surrounded the mass of bacteriocytes containing Profftella. Once fully surrounded, the bacteriocyte mass containing Profftella was fused into a syncytium. Prior to hatching, a pair of wing-like protrusions arose from both lateral sides of the bacteriome, which continued to grow throughout the nymphal stages. These findings provide a foundation for better understanding the intricate relationship between D. citri and its microbiota. Public Library of Science 2017-12-14 /pmc/articles/PMC5730177/ /pubmed/29240843 http://dx.doi.org/10.1371/journal.pone.0189779 Text en © 2017 Dan et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Dan, Hiroki
Ikeda, Naoya
Fujikami, Masaya
Nakabachi, Atsushi
Behavior of bacteriome symbionts during transovarial transmission and development of the Asian citrus psyllid
title Behavior of bacteriome symbionts during transovarial transmission and development of the Asian citrus psyllid
title_full Behavior of bacteriome symbionts during transovarial transmission and development of the Asian citrus psyllid
title_fullStr Behavior of bacteriome symbionts during transovarial transmission and development of the Asian citrus psyllid
title_full_unstemmed Behavior of bacteriome symbionts during transovarial transmission and development of the Asian citrus psyllid
title_short Behavior of bacteriome symbionts during transovarial transmission and development of the Asian citrus psyllid
title_sort behavior of bacteriome symbionts during transovarial transmission and development of the asian citrus psyllid
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5730177/
https://www.ncbi.nlm.nih.gov/pubmed/29240843
http://dx.doi.org/10.1371/journal.pone.0189779
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